IP Library Granted Patent US 9,920,033
Granted Patent B2
US 9,920,033 · App. 15/350,013 · Granted Mar 20, 2018

Crystalline form of a substituted quinoline compound and pharmaceutical compositions thereof

Inventors: Ning Xi (Newbury Park, CA); Mingming Sun (Guangdong, CN)
Assignees: Calitor Sciences, LLC; Sunshine Lake Pharma Co., LTD.
C07D401/12A61K9/0053A61K9/48A61K31/436A61K31/4709A61K38/21A61K45/06C07C309/30C07B2200/13
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Quick Facts
Patent No.
US 9,920,033
App. No.
15/350,013
Granted
Mar 20, 2018
Kind
B2
Abstract

The present invention relates to a crystalline form of N-(3-fluoro-4-((7-(2-hydroxy-2-methylpropoxy)quinolin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide p-toluenesulfonate, the process for preparing the crystalline form thereof, and the pharmaceutical compositions comprising the crystalline form thereof. This invention also relates to a method of using such a crystalline form and pharmaceutical compositions comprising the crystalline form thereof in the treatment of hyperproliferative diseases in mammals, especially in humans.

Claims (19)

1. A crystalline form of a compound of formula (I):

wherein the crystalline form is form A having:

a) an X-ray powder diffraction pattern comprising peaks, in terms of 2θ, at about 8.29°, about 9.53°, about 11.11°, about 16.99°, about 18.75° and about 23.66°; or

b) an X-ray powder diffraction pattern comprising peaks, in terms of 2θ, at 8.29°±0.2°, 9.53°±0.2°, 11.11°±0.2°, 16.99°±0.2°, 18.75°±0.2° and 23.66°±0.2°; or

c) unit cell parameters substantially equal to the following:

(i) unit cell dimensions: a=8.7430 Å, b=12.8275 Å, c=16.1281 Å, a=96.689°, β=95.737°, γ=99.649°;

(ii) space group: P-1;

(iii) volume: 1757.82 Å 3 ;

(iv) Z: 2; and

(v) calculated density: 1.377 g/cm 3 .

2. The crystalline form of claim 1 having an X-ray powder diffraction pattern comprising peaks, in terms of 2θ, at about 8.29°, about 9.53°, about 11.11°, about 15.28°, about 16.99°, about 18.75°, about 19.14°, about 19.98°, about 20.42°, about 21.77°, about 22.02° and about 23.66°, or at 8.29°±0.2°, 9.53°±0.2°, 11.11°±0.2°, 15.28°±0.2°, 16.99°±0.2° 18.75°±0.2° 19.14°±0.2° 19.98°±0.2° 20.42°±0.2° 21.77°±0.2°, 22.02°±0.2° and 23.66°±0.2°.

3. The crystalline form of claim 1 , wherein the X-ray powder diffraction pattern comprising peaks, in terms of 2θ, at about 8.29°, about 9.53°, about 11.11°, about 12.67°, about 14.04°, about 15.28°, about 15.82°, about 16.99°, about 18.75°, about 19.14°, about 19.98°, about 20.42°, about 21.77°, about 22.02°, about 22.45°, about 22.65°, about 23.66°, about 26.85°, about 27.94° and about 28.34°, or at 8.29°±0.2°, 9.53°±0.2°, 11.11°±0.2°, 12.67°±0.2°, 14.04°±0.2°, 15.28°±0.2°, 15.82°±0.2°, 16.99°±0.2°, 18.75°±0.2° 19.14°±0.2° 19.98°±0.2° 20.42°±0.2° 21.77°±0.2° 22.02°±0.2° 22.45°±0.2°, 22.65°±0.2°, 23.66°±0.2°, 26.85°±0.2°, 27.94°±0.2° and 28.34°±0.2°.

4. The crystalline form of claim 1 , wherein the X-ray powder diffraction pattern is substantially in accordance with that shown in FIG. 2 .

5. The crystalline form of claim 1 , wherein the crystalline form is substantially pure.

6. A pharmaceutical composition comprising the crystalline form of claim 1 and a pharmaceutically acceptable excipient, carrier, vehicle or a combination thereof.

7. The pharmaceutical composition of claim 6 further comprising a therapeutic agent.

8. The pharmaceutical composition of claim 7 , wherein the therapeutic agent is melphalan, cyclophosphamide, ifosfamide, busulfan, carmustine, lomustine, streptozocin, cisplatin, carboplatin, oxaliplatin, dacarbazine, temozolomide, procarbazine, methotrexate, fluorouracil, cytarabine, gemcitabine, mercaptopurine, fludarabine, vinblastine, vincristine, vinorelbine, paclitaxel, docetaxel, topotecan, irinotecan, etoposide, trabectedin, dactinomycin, doxorubicin, epirubicin, daunorubicin, mitoxantrone, bleomycin, mitomycin, ixabepilone, tamoxifen, flutamide, gonadorelin analogues, megestrol, prednisone, dexamethasone, methylprednisolone, thalidomide, interferon alfa, leucovorin, sirolimus, temsirolimus, everolimus, afatinib, alisertib, amuvatinib, apatinib, axitinib, bosutinib, bortezomib, brivanib, cediranib, cabozantinib, crenolanib, crizotinib, dabrafenib, dacomitinib, danusertib, dasatinib, dovitinib, erlotinib, foretinib, ganetespib, gefitinib, ibrutinib, icotinib, imatinib, iniparib, lapatinib, lenvatinib, linifanib, linsitinib, masitinib, momelotinib, neratinib, nilotinib, niraparib, oprozomib, olaparib, pazopanib, pegaptanib, pictilisib, ponatinib, quizartinib, radotinib, regorafenib, rigosertib, rucaparib, ruxolitinib, saracatinib, saridegib, sorafenib, sunitinib, tasocitinib, telatinib, tivantinib, tivozanib, tofacitinib, trametinib, vandetanib, veliparib, vemurafenib, vismodegib, volasertib, alemtuzumab, bevacizumab, brentuximabvedotin, catumaxomab, cetuximab, denosumab, gemtuzumab, ipilimumab, nimotuzumab, ofatumumab, panitumumab, ramucirumab, rituximab, tositumomab, trastuzumab, idelalisib, duvelisib, gilteritinib, buparlisib, taselisib, copanlisib, voxtalisib, pilaralisib, sonolisib, perifosine, alectinib, ibrutinib, pertuzumab, nintedanib, cobimetinib, temsirolimus, sirolimus, pixantrone or a combination thereof.

9. A method of treating or lessening the severity of a proliferative disorder in a patient by administering to the patient with the crystalline form of claim 1 , wherein the proliferative disorder is gastric cancer, gastric adenocarcinoma, kidney cancer, renal cell carcinoma, liver cancer, hepatocellular carcinoma or lung cancer thereof.

10. A method of treating or lessening the severity of a proliferative disorder in a patient by administering to the patient with the pharmaceutical composition of claim 6 , wherein the proliferative disorder is gastric cancer, gastric adenocarcinoma, kidney cancer, renal cell carcinoma, liver cancer, hepatocellular carcinoma or lung cancer thereof.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2021
From: CALITOR SCIENCES, LLC.
To: SUNSHINE LAKE PHARMA CO., LTD.
Reel/Frame 056177/0572 →
CORRECTIVE ASSIGNMENT TO CORRECT THE 15/961,688 PREVIOUSLY RECORDED ON REEL 052922 FRAME 0077. ASSIGNOR(S) HEREBY CONFIRMS THE THE ASSIGNMENT. Recorded Sep 29, 2020
From: NORTH & SOUTH BROTHER PHARMACY INVESTMENT COMPANY LIMITED; CALITOR SCIENCES, LLC
To: SUNSHINE LAKE PHARMA CO., LTD.; CALITOR SCIENCES LLC
Reel/Frame 053921/0538 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2020
From: NORTH & SOUTH BROTHER PHARMACY INVESTMENT COMPANY LIMITED; CALITOR SCIENCES, LLC
To: SUNSHINE LAKE PHARMA CO., LTD.; CALITOR SCIENCES LLC
Reel/Frame 052922/0077 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2019
From: SUNSHINE LAKE PHARMA CO., LTD.; CALITOR SCIENCES, LLC
To: NORTH & SOUTH BROTHER PHARMACY INVESTMENT COMPANY LIMITED; CALITOR SCIENCES, LLC
Reel/Frame 050776/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 16, 2016
From: XI, NING; SUN, MINGMING
To: SUNSHINE LAKE PHARMA CO. LTD; CALITOR SCIENCES, LLC
Reel/Frame 040634/0051 →
Continuity (2)
Provisional Application 62255391 · Nov 14, 2015
Related Publication 20170313678A1 · Nov 2, 2017